ENST00000342992.11:c.88321A>G
(TTN)
|
ENSP00000343764.6:p.Ile29441Val
|
|
ENST00000342175.11:c.69406A>G
(TTN)
|
ENSP00000340554.6:p.Ile23136Val
|
|
ENST00000359218.10:c.69205A>G
(TTN)
|
ENSP00000352154.5:p.Ile23069Val
|
|
ENST00000342175.10:c.69406A>G
(TTN)
|
ENSP00000340554.6:p.Ile23136Val
|
|
ENST00000342992.10:c.88321A>G
(TTN)
|
ENSP00000343764.6:p.Ile29441Val
|
|
ENST00000359218.9:c.69205A>G
(TTN)
|
ENSP00000352154.5:p.Ile23069Val
|
|
ENST00000460472.6:c.68830A>G
(TTN)
|
ENSP00000434586.1:p.Ile22944Val
|
|
ENST00000589042.5:c.96025A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile32009Val
|
|
ENST00000591111.5:c.91102A>G
(TTN)
|
ENSP00000465570.1:p.Ile30368Val
|
|
ENST00000615779.4:c.91102A>G
(TTN)
|
ENSP00000483597.1:p.Ile30368Val
|
|
NM_001256850.1:c.91102A>G
(TTN)
|
NP_001243779.1:p.Ile30368Val
|
|
NM_001267550.2:c.96025A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ile32009Val
|
|
NM_003319.4:c.68830A>G
(TTN)
|
NP_003310.4:p.Ile22944Val
|
|
NM_133378.4:c.88321A>G
(TTN)
|
NP_596869.4:p.Ile29441Val
|
|
NM_133432.3:c.69205A>G
(TTN)
|
NP_597676.3:p.Ile23069Val
|
|
NM_133437.4:c.69406A>G
(TTN)
|
NP_597681.4:p.Ile23136Val
|
|
NR_038271.1:n.446+20568T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1843T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.95122A>G
(TTN)
|
XP_011510031.1:p.Ile31708Val
|
|
XM_011511730.1:c.69016A>G
(TTN)
|
XP_011510032.1:p.Ile23006Val
|
|
XM_011511731.1:c.68875A>G
(TTN)
|
XP_011510033.1:p.Ile22959Val
|
|
XM_017004819.1:c.94918A>G
(TTN)
|
XP_016860308.1:p.Ile31640Val
|
|
XM_017004820.1:c.90316A>G
(TTN)
|
XP_016860309.1:p.Ile30106Val
|
|
XM_017004821.1:c.90313A>G
(TTN)
|
XP_016860310.1:p.Ile30105Val
|
|
XM_017004822.1:c.87355A>G
(TTN)
|
XP_016860311.1:p.Ile29119Val
|
|
XM_017004823.1:c.68971A>G
(TTN)
|
XP_016860312.1:p.Ile22991Val
|
|
XM_024453094.1:c.90466A>G
(TTN)
|
XP_024308862.1:p.Ile30156Val
|
|
XM_024453095.1:c.90463A>G
(TTN)
|
XP_024308863.1:p.Ile30155Val
|
|
XM_024453096.1:c.89896A>G
(TTN)
|
XP_024308864.1:p.Ile29966Val
|
|
XM_024453097.1:c.87238A>G
(TTN)
|
XP_024308865.1:p.Ile29080Val
|
|
XM_024453098.1:c.87157A>G
(TTN)
|
XP_024308866.1:p.Ile29053Val
|
|
XM_024453099.1:c.68920A>G
(TTN)
|
XP_024308867.1:p.Ile22974Val
|
|
XM_024453100.1:c.58774A>G
(TTN)
|
XP_024308868.1:p.Ile19592Val
|
|